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- 详细信息
- 文献和实验
- 技术资料
- 供应商:
上海联迈生物工程有限公司
- 库存:
大量
- 目录编号:
LM-9005R
- 克隆性:
多克隆
- 抗原来源:
Rabbit
- 保质期:
1年
- 抗体英文名:
CECR1
- 抗体名:
猫眼综合征染色体候选基因1抗体
- 宿主:
Rabbit
- 适应物种:
Human, Pig,
- 免疫原:
KLH conjugated synthetic peptide derived from human CECR1/ADGF:421-511/511
- 亚型:
IgG
- 形态:
Lyophilized or Liquid
- 应用范围:
ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 Flow-Cyt=1ug/test IF=1:50-200 (石蜡切片需做抗原修复)
- 浓度:
1mg/ml
- 保存条件:
Store at -20 °C
- 规格:
100ul 200ul
| 英文名称 | CECR1 |
| 中文名称 | 猫眼综合征染色体候选基因1抗体 |
| 别 名 | ADGF; Cat eye syndrome chromosome region candidate 1; Cat eye syndrome critical region protein 1; Cat eye syndrome critical region protein 1 precursor; CECR 1; IDGFL; CECR1_HUMAN. |
| 规格价格 | 100ul/1380元 购买 200ul/2200元 购买 大包装/询价 |
| 说 明 书 | 100ul 200ul |
| 研究领域 | 细胞生物 免疫学 表观遗传学 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Pig, |
| 产品应用 | ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 Flow-Cyt=1ug/test IF=1:50-200 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 56kDa |
| 细胞定位 | 分泌型蛋白 |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human CECR1/ADGF:421-511/511 |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
| PubMed | PubMed |
| 产品介绍 | background: CECR1 is a member of the adenosine and AMP deaminases family. It may act as a growth factor and have adenosine deaminase activity. It is a candidate gene for cat eye syndrome. Two transcript variants encoding distinct isoforms have been identified for this gene. Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterized by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects. Function: Adenosine deaminase that may contribute to the degradation of extracellular adenosine, a signaling molecule that controls a variety of cellular responses. Requires elevated adenosine levels for optimal enzyme activity. Binds to cell surfaces via proteoglycans and may play a role in the regulation of cell proliferation and differentiation, independently of its enzyme activity. Subunit: Homodimer. Interacts with adenosine receptors. Binds heparin. Subcellular Location: Secreted Tissue Specificity: Detected in blood plasma (at protein level). Widely expressed, with most abundant expression in human adult heart, lung, lymphoblasts, and placenta as well as fetal lung, liver, and kidney. In embryo, expressed in the outflow tract and atrium of the developing heart, the VII/VIII cranial nerve ganglion, and the notochord. Similarity: Belongs to the adenosine and AMP deaminases family. ADGF subfamily. SWISS: Q9NZK5 Gene ID: 51816 Database links: Entrez Gene: 51816 Human Omim: 607575 Human SwissProt: Q9NZK5 Human Unigene: 170310 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 产品图片 | ![]() Blank control: Molt4. Primary Antibody (green line): Rabbit Anti-CECR1/FITC Conjugated antibody (bs-9005R-FITC) Dilution: 1μg /10^6 cells; Isotype Control Antibody (orange line): Rabbit IgG-FITC . Protocol The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 0.1% PBST for 20 min at-20℃. The cells were then incubated in 5% BSA to block non-specific protein-protein interactions for 30 min at room temperature. The cells were stained with Primary Antibody for 30 min at room temperature. Acquisition of 20,000 events was performed. |
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文献和实验敲除这一基因,水稻、玉米可增产约 10%!中国团队最新研究登上 Science
Number, KRN) 这一性状相关的位点,其中 qKRN2 是影响最大的位点。随后,他们通过定位克隆探索了 qKRN2 影响区域的基因,有趣的是他们在该区域仅找到了一个候选基因 KRN2(Kernel rownumber 2)。这个基因与玉米上有多少排籽粒有关,因此对玉米产量有很大影响。他们后续的实验证明,KRN2 的突变可使玉米粒行数增加约 1.4 行,代表着更高的产量。 图片来源:Science KRN2 通过与 DUF1644 相互作用负向调控 KRN 为了阐明 KRN2 的分子
(genome scanning);将疾病相关位点定位于染色体某个区域,然后再行候选基因策略或连锁不平衡分析,确定致病基因位点。如果利用家系进行连锁分析,即采用定位克隆;若是利用群体样本,则应用连锁不平衡分析进行基因定位。全基因组扫描已成功地应用在许多疾病的致病相关基因克隆上,并取得了一定的成果。 全基因组扫描所利用的是在人类基因组大量存在的微卫星或SNP,虽然当前使用较多的仍是微卫星,但由于芯片技术的发展,全基因组高分布密度的商品化SNP芯片相继面世(如Affymetrix公司的10k,100
bahai 大家好,最近开始课题,有一想法,不知道是否可行,说来请大家给指点迷津,先行谢过各位! 比如,我想研究某一肿瘤,最近对一个病人的肿瘤细胞进行培养后,进行染色体核型分析发现:随即取的所有细胞的核型完全一致,而且,染色体缺失发生的地方都在相同染色体的相同部位。由此可见,至少在来自该病人的肿瘤组织经培养后的这些细胞应该是来自同一个克隆群的。 于是检索,对此肿瘤染色体核型研究的论文寥寥可数,而且都是在早年,此类研究仅仅报道发现了有染色体
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